Madeleine Duncan Brown said the same.
found this by searching "santa muerte" fren
https://kvoa.com/news/2019/12/18/digging-deeper-new-details-in-take-down-of-tucson-drug-trafficking-organization/
https://www.kgun9.com/news/local-news/ups-drug-case-police-say-severed-goat-and-cat-heads-found
Seems notable, but not a boatfag.
not just your 'tism
Randall Rutta: Discrimination against people with rare diseases
https://triblive.com/opinion/randall-rutta-discrimination-against-people-with-rare-diseases/
https://archive.is/wip/lwaYG
FDA officials approved a record number of rare disease treatments in 2018. One groundbreaking medicine treats an inherited bone condition that causes intense pain and immobility. Another treats Fabry disease, a genetic condition that can lead to kidney failure or stroke.
Breakthroughs like these offer hope to 30 million Americans living with rare diseases. But there’s still a long way to go. Scientists estimate there are 7,000 rare diseases, each of which afflicts fewer than 200,000 people. The majority of these ailments — 95% — lack a single approved treatment.
Unfortunately, one prominent health care nonprofit could undermine research into rare diseases.
The group, the Institute for Clinical and Economic Review (ICER), analyzes the “cost-effectiveness” of many new FDA-approved drugs, including treatments for rare diseases. Because it relies on flawed assumptions, ICER mostly concludes that rare disease treatments aren’t worth the price….
HABBY BIRTHDAY DAN!
Thanks for all you do.